Results 131 to 140 of about 341,590 (292)

Wound, pressure ulcer, and burn guidelines (2023)―4: Guidelines for the management of connective tissue disease/vasculitis‐associated skin ulcers, third edition

The Journal of Dermatology, Volume 52, Issue 6, Page e430-e480, June 2025.
Yoshihide Asano, Jun Asai, Takayuki Ishii, Yohei Iwata, Masanari Kodera, Chie Miyabe, Akihiko Uchiyama, Youichi Ogawa, Ken Okamura, Mari Kishibe, Yuta Koike, Yorihisa Kotobuki, Noriki Fujimoto, Takuya Miyagi, Yukie Yamaguchi, Ayumi Yoshizaki, Reiko Omori, Takeshi Nakanishi, Hiroshi Fujiwara, Takeo Maekawa, Sei‐ichiro Motegi, Yuichiro Yoshino, Minoru Hasegawa, Manabu Fujimoto, Takao Tachibana, Wound, Pressure Ulcer, and Burn Guidelines Drafting Committee (connective tissue disease/vasculitis group)   +27 more
wiley   +1 more source

Molecular mechanisms in idiopathic inflammatory myopathies [PDF]

, 2014
Background: Myositis is a group of rare autoimmune diseases. Muscle weakness and fatigue are the dominant symptoms and inflammation with T cells and macrophages is a characteristic finding in muscle tissue.
Zong, Mei
core   +1 more source

Drug treatment of juvenile dermatomyositis. [PDF]

, 1983
Gopika D. Miller, J Z Heckmatt, Victor Dubowitz   +2 more
openalex   +1 more source

Role of mitochondria in the myopathy of juvenile dermatomyositis and implications for skeletal muscle calcinosis

Journal of Autoimmunity, 2023
Bhargavi Duvvuri, L. Pachman, Payton Hermanson, Ting Wang, Richard L. Moore, Dennis Ding-Hwa Wang, Aaron Long, Gabrielle Morgan, Stephen Doty, R. Tian, Y. Sancak, C. Lood   +11 more
semanticscholar   +1 more source

Atypical presentation of anti-NXP-2 positive juvenile dermatomyositis

Revista da Sociedade Portuguesa de Dermatologia e Venereologia, 2023
Dear Editor, The anti-NXP-2 is one of a myositis-specific autoantibody considered a marker of dermatomyositis (DM)1,2. In addition, there is a strong relationship between NXP-2 autoantibodies and calcinosis, particularly in juvenile DM2.
Andreia Coimbra-Sousa, Renata Miossi, Fernando H. C. de Souza, Samuel Katsuyuki-Shinjo   +3 more
doaj  

Genetic association study of NF-κB genes in UK Caucasian adult and juvenile onset idiopathic inflammatory myopathy [PDF]

, 2012
Treatment-resistant muscle wasting is an increasingly recognized problem in idiopathic inflammatory myopathy (IIM). TNF-α is thought to induce muscle catabolism via activation of nuclear factor-kappa B (NF-κB). Several genes share homology with the NF-κB
Betteridge, Z, Chinoy, H, Cooper, RG, Fertig, N, Gunawardena, H, Li, CK, McHugh, NJ, Oddis, CV, Ollier, WE, Platt, H, UK Adult Onset Myositis Immunogenetic Consortium and UK Juvenile, Varsani, H, Wedderburn, LR   +12 more
core  

Immunogenetic studies of juvenile dermatomyositis [PDF]

, 1983
Jan M. Friedman, Lauren M. Pachman, M. L. Maryjowski, Olga Jonasson, Norma D. Battles, William Crowe, C W Fink, Virgil Hanson, Joseph E. Levinson, Charles H. Spencer, Donita B. Sullivan   +10 more
openalex   +1 more source

Juvenile Dermatomyositis with Generalized Edema

Pediatric Neurology Briefs, 2001
A 7-year-old girl presenting with an 8-week history of fatigue, myalgia, dyspnea, and generalized, nonpitting edema of the extremities, face, chest, and abdomen, is reported from the Walter Reed Army Medical Center, Washington, DC.
J Gordon Millichap
doaj   +1 more source

Radiological conference. Juvenile rheumatoid arthritis [PDF]

, 1997
published_or_final_versio
Peh, WCG
core  

Pharmacological management of dermatomyositis [PDF]

, 2018
K
Dankó, Katalin, Griger, Zoltán, Nagy-Vincze, Melinda   +2 more
core   +1 more source